Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Allofix Insertion Kit Recalled by Musculoskeletal Transplant Foundation, Inc. Due to Musculoskeletal Transplant Foundation is recalling a certain lot...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Musculoskeletal Transplant Foundation, Inc. directly.
Affected Products
Allofix Insertion Kit, 2.0 mm, Single Drill, Product Usage: MTF Surgical Instruments are designed for the specific needs of the orthopedic surgeon and are intended to be used in conjunction with the associated allograft. This kit is for single use only.
Quantity: 117 units
Why Was This Recalled?
Musculoskeletal Transplant Foundation is recalling a certain lot of Allofix Insertion Kits because they are labeled as having a 2.0mm diameter drill however it may contain a 2.4 mm diameter drill.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Musculoskeletal Transplant Foundation, Inc.
Musculoskeletal Transplant Foundation, Inc. has 9 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report